Details
Stereochemistry | ACHIRAL |
Molecular Formula | C21H20Cl2FN3O2 |
Molecular Weight | 436.307 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=C(C=C1)C2=C(CCN3CCN(CC3)C4=CC(Cl)=CC(Cl)=C4)OC(=O)N2
InChI
InChIKey=VIASEBSYVIYYEZ-UHFFFAOYSA-N
InChI=1S/C21H20Cl2FN3O2/c22-15-11-16(23)13-18(12-15)27-9-7-26(8-10-27)6-5-19-20(25-21(28)29-19)14-1-3-17(24)4-2-14/h1-4,11-13H,5-10H2,(H,25,28)
Molecular Formula | C21H20Cl2FN3O2 |
Molecular Weight | 436.307 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/2571727
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2571727
Lodiperon exhibited neuroleptic activity with very low liability to the extrapyramidal side effects. Its activity was greater than that of butropipazone and fluanisone, while of the same order of that of chlorpromazine; however, lodiperon showed a longer lasting activity and minor ability to produce catalepsy as compared with the reference drugs.
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:35:22 GMT 2023
by
admin
on
Fri Dec 15 15:35:22 GMT 2023
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Record UNII |
T8593BT7B4
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C28197
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100000082017
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T8593BT7B4
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CHEMBL73383
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C66025
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Related Record | Type | Details | ||
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ACTIVE MOIETY |